Nickel-Catalyzed Cross-Coupling of Anisoles with Alkyl Grignard Reagents via C–O Bond Cleavage-Reference-Cited by-同舟云学术

Nickel-Catalyzed Cross-Coupling of Anisoles with Alkyl Grignard Reagents via C–O Bond Cleavage

Published:2015-08-27 Issue:17 Volume:17 Page:4352-4355
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Tobisu Mamoru¹,Takahira Tsuyoshi¹,Chatani Naoto¹

Affiliation:

1. Department of Applied Chemistry, Faculty of Engineering and ‡Center for Atomic and Molecular Technologies, Graduate School of Engineering, Osaka University, Suita, Osaka 565-0871, Japan

Funder

Ministry of Education, Culture, Sports, Science, and Technology

Japan Science and Technology Agency

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.5b02200

Reference63 articles.

1. Selective carbon-carbon bond formation by cross-coupling of Grignard reagents with organic halides. Catalysis by nickel-phosphine complexes

2. Activation of Grignard reagents by transition-metal complexes. A new and simple synthesis of trans-stilbenes and polyphenyls

3. Some applications of the Grignard cross-coupling reaction in the industrial field

4. Preparation of 4-Allylisoindoline via a Kumada Coupling with Allylmagnesium Chloride

5. Investigation of a Kumada Cross Coupling Reaction for Large-Scale Production of (2S, 7R, E)-2-Isopropyl-7-(4-methoxy-3-(3-methoxypropoxy)benzyl)-N,N,8-trimethylnon-4-enamide

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